Variant report

Variant	rs4413578
Chromosome Location	chr6:75753342-75753343
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs11754104	0.94[AFR][1000 genomes];0.90[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs11758551	0.92[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs11758990	0.85[EUR][1000 genomes]
rs4560603	0.84[EUR][1000 genomes]
rs4569931	0.94[AFR][1000 genomes];0.88[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs4571524	0.84[EUR][1000 genomes]
rs56310973	0.91[AFR][1000 genomes];0.88[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs6453809	0.84[EUR][1000 genomes]
rs6928356	0.80[EUR][1000 genomes]
rs73462024	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes]

No data

Chromatin state (count:1 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:75753200-75758000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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